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Cited 36 time in webofscience Cited 38 time in scopus
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Total Synthesis of (+/-)-Lycorine from the Endo-Cycloadduct of 3,5-Dibromo-2-pyrone and (E)-beta-Borylstyrene

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dc.contributor.authorShin, Hyeong-Seob-
dc.contributor.authorJung, Yong-Geun-
dc.contributor.authorCho, Hyun-Kyu-
dc.contributor.authorPark, Yong-Gyu-
dc.contributor.authorCho, Cheon-Gyu-
dc.date.accessioned2022-07-07T05:00:26Z-
dc.date.available2022-07-07T05:00:26Z-
dc.date.issued2014-11-
dc.identifier.issn1523-7060-
dc.identifier.issn1523-7052-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/143300-
dc.description.abstractA new synthetic route to (+/-)-lycorine, starting from the endo-cycloadduct of 3,5-dibromo-2-pyrone and (E)-beta-borylstyrene, is reported. Boronate oxidation and a set of reactions including face-selective epoxidation provided the pivotal C1-OH group and C3/C3a double bond.-
dc.format.extent3-
dc.language영어-
dc.language.isoENG-
dc.publisherAmerican Chemical Society-
dc.titleTotal Synthesis of (+/-)-Lycorine from the Endo-Cycloadduct of 3,5-Dibromo-2-pyrone and (E)-beta-Borylstyrene-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1021/ol502792p-
dc.identifier.scopusid2-s2.0-84910022297-
dc.identifier.wosid000344635200054-
dc.identifier.bibliographicCitationOrganic Letters, v.16, no.21, pp 5718 - 5720-
dc.citation.titleOrganic Letters-
dc.citation.volume16-
dc.citation.number21-
dc.citation.startPage5718-
dc.citation.endPage5720-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalWebOfScienceCategoryChemistry, Organic-
dc.subject.keywordPlusDIELS-ALDER REACTION-
dc.subject.keywordPlusAMARYLLIDACEAE ALKALOIDS-
dc.subject.keywordPlusBIOLOGICAL EVALUATION-
dc.subject.keywordPlusLYCORINE DERIVATIVES-
dc.subject.keywordPlus(+/-)-CRININE-
dc.subject.keywordPlusCONCISE-
dc.subject.keywordPlusCASCADE-
dc.subject.keywordPlusROUTE-
dc.identifier.urlhttps://pubs.acs.org/doi/10.1021/ol502792p-
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